Cervitec F
K-Number: K191453 · 2020-02-11
ApplicantIvoclar Vivadent, AG
Decision Date2020-02-11
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Cervitec F is a medical device manufactured by Ivoclar Vivadent, AG. It received FDA 510(k) clearance on 2020-02-11 under approval number K191453. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Cervitec F?
Cervitec F is a medical device that received FDA 510(k) clearance on 2020-02-11. It is manufactured by Ivoclar Vivadent, AG. The 510(k) number is K191453.
When was Cervitec F approved by the FDA?
Cervitec F received FDA 510(k) clearance on 2020-02-11, under approval number K191453.
What company makes Cervitec F?
Cervitec F is manufactured by Ivoclar Vivadent, AG.
What is the FDA product code for Cervitec F?
The FDA product code for Cervitec F is LBH.
Other Devices by Ivoclar Vivadent, AG
Related Devices (Code: LBH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.